Package 43547-398-01

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 43547-398-01
Digits Only 4354739801
Product NDC 43547-398
Product ID 43547-398_d8ce29b2-7f3a-4944-bf9e-0fcebb25d3c4
Description

10 TABLET in 1 BOTTLE, PLASTIC (43547-398-01)

Marketing

Marketing Status
Marketed Since 2002-03-29
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d8ce29b2-7f3a-4944-bf9e-0fcebb25d3c4", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0343547397036"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798"], "spl_set_id": ["60c97ab9-b25e-4ea5-a159-792292178c65"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Solco Healthcare U.S., LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (43547-398-01)", "package_ndc": "43547-398-01", "marketing_start_date": "20020329"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43547-398-03)", "package_ndc": "43547-398-03", "marketing_start_date": "20020329"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (43547-398-05)", "package_ndc": "43547-398-05", "marketing_start_date": "20020329"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43547-398-10)", "package_ndc": "43547-398-10", "marketing_start_date": "20020329"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (43547-398-11)", "package_ndc": "43547-398-11", "marketing_start_date": "20020329"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (43547-398-50)", "package_ndc": "43547-398-50", "marketing_start_date": "20020329"}], "brand_name": "Hydrochlorothiazide", "product_id": "43547-398_d8ce29b2-7f3a-4944-bf9e-0fcebb25d3c4", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "43547-398", "generic_name": "Hydrochlorothiazide", "labeler_name": "Solco Healthcare U.S., LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040412", "marketing_category": "ANDA", "marketing_start_date": "20020329", "listing_expiration_date": "20261231"}